Canonical Allele Identifier: CA2576001385

Gene: NUP93

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.56836770G>A , CM000678.2:g.56836770G>A	GRCh38
NC_000016.9:g.56870682G>A , CM000678.1:g.56870682G>A	GRCh37
NC_000016.8:g.55428183G>A	NCBI36
NG_052904.1:g.111666G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308159.10:c.1899+53G>A MANE Select	ENSP00000310668.5:n.1899+53G>A
ENST00000308159.9:c.1899+53G>A	ENSP00000310668.5:n.1899+53G>A
ENST00000542526.5:c.1530+53G>A	ENSP00000440235.1:n.1530+53G>A
ENST00000563405.1:c.93+53G>A	ENSP00000458078.1:n.93+53G>A
ENST00000564887.5:c.1530+53G>A	ENSP00000458039.1:n.1530+53G>A
ENST00000569842.5:c.1899+53G>A	ENSP00000458101.1:n.1899+53G>A
NM_001242795.1:c.1530+53G>A	NP_001229724.1:n.1530+53G>A
NM_001242796.1:c.1530+53G>A	NP_001229725.1:n.1530+53G>A
NM_014669.4:c.1899+53G>A	NP_055484.3:n.1899+53G>A
XM_005256263.2:c.1899+53G>A	XP_005256320.1:n.1899+53G>A
NM_001242796.2:c.1530+53G>A	NP_001229725.1:n.1530+53G>A
XM_005256263.3:c.1899+53G>A	XP_005256320.1:n.1899+53G>A
NM_014669.5:c.1899+53G>A MANE Select	NP_055484.3:n.1899+53G>A
NM_001242795.2:c.1530+53G>A	NP_001229724.1:n.1530+53G>A